Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of AnsellLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Ansell Pacific with 2 510(k) clearances. The most recent is a 510(k) clearance dated Jul 14, 1989: PATIENT EXAMINATION GLOVES (LATEX).
| Jul 14, 1989 | PATIENT EXAMINATION GLOVES (LATEX)K892570 · LYY | 510(k) clearances |
| Jul 14, 1989 | ANATOMICAL EXAMINATION GLOVESK892579 · LYY | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built